eudamed_udi
Primary ID: 04046678002409
Simplex (UDI 04046678002409)
Manufactured by REBOTEC Rehabilitationsmittel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Simplex - Primary ID 04046678002409
Device Regulatory Overview
The Simplex (Model/Catalog Number: 13310) is a medical device manufactured by REBOTEC Rehabilitationsmittel GmbH. This product is indexed under FDA Product Code / Category Classification Y120399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13310
- Product Code / EMDN
- Y120399
- Device Name
- Gehstöcke
- Database Sync Date
- 2026-08-09 16:45:59
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Simplex?
The registered manufacturer of record for Simplex is REBOTEC Rehabilitationsmittel GmbH.
What is the Primary UDI-DI identifier for Simplex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046678002409.
What classification code is assigned to this device?
This device is registered under product classification code Y120399.
Similar Classification Devices (Y120399)
Other Devices by REBOTEC Rehabilitationsmittel GmbH
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